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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1949 1
1955 1
1956 1
1957 1
1959 2
1961 2
1962 2
1964 1
1965 1
1966 2
1967 2
1969 3
1970 2
1971 1
1974 2
1975 3
1976 4
1977 8
1978 8
1979 4
1980 6
1981 7
1982 5
1983 10
1984 11
1985 16
1986 11
1987 25
1988 23
1989 23
1990 16
1991 17
1992 31
1993 27
1994 28
1995 19
1996 6
1997 6
1998 6
1999 8
2000 7
2001 6
2002 22
2003 19
2004 13
2005 7
2006 6
2007 11
2008 6
2009 17
2010 10
2011 3
2012 2
2013 2
2014 2
2015 1
2016 1
2018 2
2020 1
2021 1
2022 1
2024 0

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Article type

Publication date

PubMed (OMIM) for id: 1756

476 results

Results by year

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Page 1
TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy.
Spitali P, Zaharieva I, Bohringer S, Hiller M, Chaouch A, Roos A, Scotton C, Claustres M, Bello L, McDonald CM, Hoffman EP; CINRG Investigators; Koeks Z, Eka Suchiman H, Cirak S, Scoto M, Reza M, 't Hoen PAC, Niks EH, Tuffery-Giraud S, Lochmüller H, Ferlini A, Muntoni F, Aartsma-Rus A. Spitali P, et al. Eur J Hum Genet. 2020 Jun;28(6):815-825. doi: 10.1038/s41431-019-0563-6. Epub 2020 Jan 2. Eur J Hum Genet. 2020. PMID: 31896777 Free PMC article.
Cathepsin S Contributes to the Pathogenesis of Muscular Dystrophy in Mice.
Tjondrokoesoemo A, Schips TG, Sargent MA, Vanhoutte D, Kanisicak O, Prasad V, Lin SC, Maillet M, Molkentin JD. Tjondrokoesoemo A, et al. J Biol Chem. 2016 May 6;291(19):9920-8. doi: 10.1074/jbc.M116.719054. Epub 2016 Mar 10. J Biol Chem. 2016. PMID: 26966179 Free PMC article.
Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype.
Vieira NM, Elvers I, Alexander MS, Moreira YB, Eran A, Gomes JP, Marshall JL, Karlsson EK, Verjovski-Almeida S, Lindblad-Toh K, Kunkel LM, Zatz M. Vieira NM, et al. Cell. 2015 Nov 19;163(5):1204-1213. doi: 10.1016/j.cell.2015.10.049. Epub 2015 Nov 12. Cell. 2015. PMID: 26582133 Free PMC article.
Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age.
Mercier S, Toutain A, Toussaint A, Raynaud M, de Barace C, Marcorelles P, Pasquier L, Blayau M, Espil C, Parent P, Journel H, Lazaro L, Andoni Urtizberea J, Moerman A, Faivre L, Eymard B, Maincent K, Gherardi R, Chaigne D, Ben Yaou R, Leturcq F, Chelly J, Desguerre I. Mercier S, et al. Eur J Hum Genet. 2013 Aug;21(8):855-63. doi: 10.1038/ejhg.2012.269. Epub 2013 Jan 9. Eur J Hum Genet. 2013. PMID: 23299919 Free PMC article.
476 results